Canonical Allele Identifier: CA97484498

Gene: TMEM165

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55396352C>G , CM000666.2:g.55396352C>G	GRCh38
NC_000004.11:g.56262519C>G , CM000666.1:g.56262519C>G	GRCh37
NC_000004.10:g.55957276C>G	NCBI36
NG_032881.1:g.5440C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_018475.5:c.163C>G MANE Select	NP_060945.2:p.Pro55Ala
ENST00000381334.10:c.163C>G MANE Select	ENSP00000370736.5:p.Pro55Ala
NM_018475.4:c.163C>G	NP_060945.2:p.Pro55Ala
NR_073070.1:n.440C>G
NR_073070.2:n.396C>G
ENST00000381334.9:c.163C>G	ENSP00000370736.5:p.Pro55Ala
ENST00000506198.5:c.163C>G	ENSP00000425449.1:p.Pro55Ala
ENST00000508404.5:c.163C>G	ENSP00000422639.1:p.Pro55Ala
ENST00000514070.1:n.102C>G
XM_011534394.1:c.163C>G	XP_011532696.1:p.Pro55Ala
XM_011534394.3:c.163C>G	XP_011532696.1:p.Pro55Ala
XM_017008412.1:c.-283C>G	XP_016863901.1:n.-283C>G
XR_001741287.2:n.700C>G